UNIVERSAL DYNASPLINT— 510(k) K822767

Substantially Equivalent

Dynasplint Systems, Inc.

FDA 510(k) clearance K822767 for UNIVERSAL DYNASPLINT, Substantially Equivalent on 1982-10-06. Applicant: Dynasplint Systems, Inc.. Device class: 1.

Clearance details

Applicant: Dynasplint Systems, Inc.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1982-09-14
Decision date: 1982-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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